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Page 1
Fosdenopterin: First Approval.
Kang C. Kang C. Drugs. 2021 Jun;81(8):953-956. doi: 10.1007/s40265-021-01520-2. Drugs. 2021. PMID: 33909276 Review.
Fosdenopterin (Nulibry(TM)) is a synthetic cyclic pyranopterin monophosphate that is being developed by Origin Biosciences (a subsidiary of BridgeBio Pharma) for the treatment of molybdenum cofactor deficiency (MoCD) type A. ...This article summarizes the milestones
Fosdenopterin (Nulibry(TM)) is a synthetic cyclic pyranopterin monophosphate that is being developed by Origin Biosciences (a
Regulatory news: Nulibry (fosdenopterin) approved to reduce the risk of mortality in patients with molybdenum cofactor deficiency type A: FDA approval summary.
Farrell S, Karp J, Hager R, Wang Y, Adeniyi O, Wang J, Li L, Ma L, Peretz J, Summan M, Kong N, White M, Pacanowski M, Price D, Filie J, Donohue K, Joffe H. Farrell S, et al. J Inherit Metab Dis. 2021 Sep;44(5):1085-1087. doi: 10.1002/jimd.12421. Epub 2021 Aug 8. J Inherit Metab Dis. 2021. PMID: 34337775 Review. No abstract available.
Molybdenum cofactor deficiency.
Atwal PS, Scaglia F. Atwal PS, et al. Mol Genet Metab. 2016 Jan;117(1):1-4. doi: 10.1016/j.ymgme.2015.11.010. Epub 2015 Nov 25. Mol Genet Metab. 2016. PMID: 26653176 Review.
We review MoCD and focus on describing the currently published evidence of this exciting new therapeutic option for MoCD type A caused by pathogenic variants in MOCD1....
We review MoCD and focus on describing the currently published evidence of this exciting new therapeutic option for MoCD type A cause …
The molybdenum cofactor.
Mendel RR. Mendel RR. J Biol Chem. 2013 May 10;288(19):13165-72. doi: 10.1074/jbc.R113.455311. Epub 2013 Mar 28. J Biol Chem. 2013. PMID: 23539623 Free PMC article. Review.
Molybdenum Cofactor Deficiency in Humans.
Johannes L, Fu CY, Schwarz G. Johannes L, et al. Molecules. 2022 Oct 14;27(20):6896. doi: 10.3390/molecules27206896. Molecules. 2022. PMID: 36296488 Free PMC article. Review.
In the absence of a specific treatment for MoCD type B/C and SOX deficiency, we summarize recent progress in our understanding of the underlying metabolic changes in cysteine homeostasis and propose novel therapeutic interventions to circumvent those pathological changes.. …
In the absence of a specific treatment for MoCD type B/C and SOX deficiency, we summarize recent progress in our understanding of the underl …
The biosynthesis of the molybdenum cofactors.
Mendel RR, Leimkühler S. Mendel RR, et al. J Biol Inorg Chem. 2015 Mar;20(2):337-47. doi: 10.1007/s00775-014-1173-y. Epub 2014 Jul 1. J Biol Inorg Chem. 2015. PMID: 24980677
Insights into the Cnx1E catalyzed MPT-AMP hydrolysis.
Hercher TW, Krausze J, Hoffmeister S, Zwerschke D, Lindel T, Blankenfeldt W, Mendel RR, Kruse T. Hercher TW, et al. Biosci Rep. 2020 Jan 31;40(1):BSR20191806. doi: 10.1042/BSR20191806. Biosci Rep. 2020. PMID: 31860061 Free PMC article.
Successful treatment of molybdenum cofactor deficiency type A with cPMP.
Veldman A, Santamaria-Araujo JA, Sollazzo S, Pitt J, Gianello R, Yaplito-Lee J, Wong F, Ramsden CA, Reiss J, Cook I, Fairweather J, Schwarz G. Veldman A, et al. Pediatrics. 2010 May;125(5):e1249-54. doi: 10.1542/peds.2009-2192. Epub 2010 Apr 12. Pediatrics. 2010. PMID: 20385644
12 results